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Updated: Jun 26, 2025

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells
Published on: May 6, 2018
Participation of suicide gene extracellular vesicles in metastasis prevention
Dajana Vanova1, Michal Andrezal1, Jana Jakubechova1
1Stem Cell Preparation Department, St. Elisabeth Cancer Institute, Bratislava, Slovakia.
Abstract:
The incidence of distant metastases is associated with most cancer-related mortalities. Extracellular vesicles (EVs), secreted from tumors and cancer-associated fibroblasts, are involved in the metastatic process mediating their organotropism through their involvement in the pre-metastatic niche formation. We have been developing suicide gene therapy mediated by EVs secreted from mesenchymal stem/ stromal cells, tumor cells, and cancer-associated fibroblasts. Suicide gene EVs conjugated with prodrug are tumor tropic, penetrate tumor cells, and kill them by intracellular conversion of nontoxic prodrug to an efficient anti-cancer drug. Here, we discuss findings regarding the possibility of using suicide gene EVs as a novel therapeutic approach for metastases, via pre-metastatic niche modification. The suicide gene EVs provide a future perspective for metastasis prevention.
Insights
Extracellular vesicles (EVs) carrying suicide genes can be engineered to target tumors, convert prodrugs into anti-cancer drugs, and prevent metastasis. This novel suicide gene therapy approach offers a promising strategy for combating cancer spread.
Area of Science:
- Oncology
- Gene Therapy
- Nanomedicine
Background:
- Distant metastases are a primary cause of cancer mortality.
- Extracellular vesicles (EVs) play a crucial role in metastasis and pre-metastatic niche formation.
- Current therapeutic strategies face challenges in effectively targeting metastatic disease.
Purpose of the Study:
- To explore the potential of suicide gene therapy mediated by extracellular vesicles (EVs) for treating cancer metastasis.
- To investigate the use of engineered EVs for pre-metastatic niche modification and metastasis prevention.
Main Methods:
- Developing suicide gene therapy using EVs derived from mesenchymal stem/stromal cells, tumor cells, and cancer-associated fibroblasts.
- Conjugating suicide genes with prodrugs for targeted delivery and intracellular activation within tumor cells.
- Evaluating the tumor-tropic nature and anti-cancer efficacy of these engineered EVs.
Main Results:
- Suicide gene EVs demonstrate tumor tropism and penetrate tumor cells effectively.
- Intracellular conversion of prodrugs by suicide gene EVs yields potent anti-cancer drugs.
- Engineered EVs show potential in modifying the pre-metastatic niche.
Conclusions:
- Suicide gene EVs represent a novel therapeutic approach for metastasis.
- This strategy holds promise for preventing cancer spread and improving patient outcomes.
- Further research into suicide gene EVs could revolutionize cancer treatment.
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